Search results for "Catalysis"

showing 10 items of 5944 documents

Preparation of a Series of “Ru(p-cymene)” Complexes with Different N-Heterocyclic Carbene Ligands for the Catalytic β-Alkylation of Secondary Alcohol…

2008

A series of five different “(p-cymene)Ru(NHC)” complexes (NHC = imidazolin-2-ylidene, imidazolin-4-ylidene, and pyrazolin-3-ylidene) have been obtained and fully characterized. The crystal structure of two of the new complexes has been determined by X-ray diffraction methods. All five complexes have been tested in the catalytic β-alkylation of secondary alcohols with primary alcohols and the dimerization of phenylacetylene, showing an excellent activity in both processes. A clear improvement on the catalytic activity of the complexes is observed when the more basic NHC ligands are used. The pyrazolylidene-Ru complex lies among the best catalysts for the β-alkylation of secondary alcohols re…

p-CymeneTransition metal carbene complexOrganic ChemistryCrystal structureAlkylationMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryPhenylacetyleneOrganic chemistryPhysical and Theoretical ChemistryCarbeneOrganometallics
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Oncogenic BRAF and p53 Interplay in Melanoma Cells and the Effects of the HDAC Inhibitor ITF2357 (Givinostat)

2023

Oncogenic BRAF mutations have been widely described in melanomas and promote tumour progression and chemoresistance. We previously provided evidence that the HDAC inhibitor ITF2357 (Givinostat) targets oncogenic BRAF in SK-MEL-28 and A375 melanoma cells. Here, we show that oncogenic BRAF localises to the nucleus of these cells, and the compound decreases BRAF levels in both the nuclear and cytosolic compartments. Although mutations in the tumour suppressor p53 gene are not equally frequent in melanomas compared to BRAF, the functional impairment of the p53 pathway may also contribute to melanoma development and aggressiveness. To understand whether oncogenic BRAF and p53 may cooperate, a po…

p53HDAC inhibitor; ITF2357; BRAF; melanoma; p53; apoptosisOrganic ChemistryapoptosisGeneral MedicineCatalysisComputer Science ApplicationsBRAFInorganic ChemistryHDAC inhibitorSettore BIO/10 - BiochimicaITF2357melanomaPhysical and Theoretical ChemistryMolecular BiologySpectroscopy
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Feedback and Communication in Active Hydrogel Spheres with pH Fronts: Facile Approaches to Grow Soft Hydrogel Structures

2021

Abstract Compartmentalized reaction networks regulating signal processing, communication and pattern formation are central to living systems. Towards achieving life‐like materials, we compartmentalized urea‐urease and more complex urea‐urease/ester‐esterase pH‐feedback reaction networks into hydrogel spheres and investigate how fuel‐driven pH fronts can be sent out from these spheres and regulated by internal reaction networks. Membrane characteristics are installed by covering urease spheres with responsive hydrogel shells. We then encapsulate the two networks (urea‐urease and ester‐esterase) separately into different hydrogel spheres to devise communication, pattern formation and attracti…

pH feedback system540 Chemistry and allied sciencesSystems ChemistrySupramolecular chemistry3D printingPattern formationlife-like systemsNanotechnology010402 general chemistry01 natural sciencessupramolecular chemistryCatalysisResearch Articleshydrogels010405 organic chemistrybusiness.industrychemical reaction networksGeneral MedicineGeneral ChemistrySoft materials0104 chemical sciencesLiving systems540 ChemieSelf-healing hydrogelsSPHERESAlginate hydrogelbusinessResearch ArticleAngewandte Chemie International Edition
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Reproducibility in Electroorganic Synthesis—Myths and Misunderstandings

2021

Abstract The use of electric current as a traceless activator and reagent is experiencing a renaissance. This sustainable synthetic method is evolving into a hot topic in contemporary organic chemistry. Since researchers with various scientific backgrounds are entering this interdisciplinary field, different parameters and methods are reported to describe the experiments. The variation in the reported parameters can lead to problems with the reproducibility of the reported electroorganic syntheses. As an example, parameters such as current density or electrode distance are in some cases more significant than often anticipated. This Minireview provides guidelines on reporting electrosyntheti…

parameterscathodeReproducibilityanodesynthesisElectroorganic Chemistry010405 organic chemistryComputer scienceThe RenaissanceMinireviewsGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceselectrochemistryMinireviewBiochemical engineeringAngewandte Chemie International Edition
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Mukaiyama-Michael reactions with α-substituted acroleins - a useful tool for the synthesis of the pectenotoxins and other natural product targets

2013

pektenotoksiini25-diphenylpyrrolidinepectenotoxinMukaiyama-Michael reactionorganocatalysistotal synthesisluonnonaineetreaktiomekanismitmyrkylliset aineet
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Isolation of Four Lytic Phages Infecting Klebsiella pneumoniae K22 Clinical Isolates from Spain

2020

This article belongs to the Special Issue Bacteriophage—Molecular Studies.

phage therapyPhage therapyPhage therapyKlebsiella pneumoniae<i>Klebsiella pneumoniae</i>medicine.medical_treatmentGenome ViralArticleHost SpecificityCatalysisMicrobiologylcsh:ChemistryInorganic ChemistryBacteriophageViral Proteins03 medical and health sciencesPodoviridaeProtein DomainsbacteriophagemedicineHumansBacteriophagesTypingPhysical and Theoretical ChemistryBacteriophagelcsh:QH301-705.5Molecular BiologyPhylogenySpectroscopy030304 developmental biologyWhole genome sequencingInfectivityLikelihood Functions0303 health sciencesbiology030306 microbiologyOrganic ChemistryGeneral Medicinebiology.organism_classification3. Good healthComputer Science ApplicationsKlebsiella pneumoniaelcsh:Biology (General)lcsh:QD1-999Lytic cycleSpainInternational Journal of Molecular Sciences
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New Evidence of the Enhanced Elimination of a Persistent Drug Used as a Lipid Absorption Inhibitor by Advanced Oxidation with UV-A and Nanosized Cata…

2019

This work demonstrates new evidence of the efficient destruction and mineralization of an emergent organic pollutant using UV-A and titanium nanosized catalysts. The target compound considered in this work is the primary metabolite of a lipid regulator drug, clofibrate, identified in many studies as refractory during conventional wastewater treatment. The photocatalytic performance study was carried out in batch mode at laboratory scale, in aqueous suspension. Kinetic data showed that titanium dioxide P25 Aeroxide® exhibits the highest photocatalytic efficiency compared to the other investigated catalysts. Pollutant degradation and mineralization efficiencies strongly increased when decreas…

pharmaceutic compoundschemistry.chemical_elementtitania catalysts02 engineering and technology010501 environmental scienceslcsh:Chemical technology01 natural sciencesCatalysisCatalysislcsh:Chemistrychemistry.chemical_compoundlcsh:TP1-1185mineralizationPhysical and Theoretical Chemistryemerging water pollutants0105 earth and related environmental sciencesdegradationPollutantQuenching (fluorescence)[SDE.IE]Environmental Sciences/Environmental Engineeringtoxicity[CHIM.CATA]Chemical Sciences/CatalysisMineralization (soil science)021001 nanoscience & nanotechnology6. Clean waterlcsh:QD1-999chemistry13. Climate actionkineticsTitanium dioxidePhotocatalysisDegradation (geology)[CHIM.OTHE]Chemical Sciences/Other0210 nano-technologyphotocatalysisNuclear chemistryTitaniumCatalysts
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Effect of Gold(I) on the Room-Temperature Phosphorescence of Ethynylphenanthrene.

2020

The synthesis of two series of gold(I) complexes containing the general formulae PR 3 ‐Au‐C≡C‐phenanthrene (PR 3 = PPh 3 ( 1a / 2a ), PMe 3 ( 1b / 2b ), PNaph 3 ( 1c / 2c )) or (diphos)(Au‐C≡C‐phenanthrene) 2 (diphos = 1,1‐ bis (diphenylphosphino)methane, dppm ( 1d / 2d ); 1,4‐ bis (diphenylphosphino)butane, dppb ( 1e / 2e )) have been synthesized. The two series differ on the position of the alkynyl substituent on the phenanthrene chromophore, being at the 9‐position (9‐ethynylphenanthrene) for the L1 ‐series and at the 2‐position (2‐ethynylphenanthrene) for the L2 ‐series. The compounds have been fully characterized by 1 H and 31 P NMR and IR spectroscopy, mass spectrometry and single cry…

phenanthreneorganic matrixesSubstituentInfrared spectroscopyOr010402 general chemistryMass spectrometry01 natural scienceskultaCatalysischemistry.chemical_compoundheavy atom effectroom temperature phosphorescence (RTP)010405 organic chemistryChemistryPhosphorescenceluminesenssiOrganic ChemistryButanekompleksiyhdisteetGeneral ChemistryChromophoreFluorescence0104 chemical sciencesPhysical chemistryFosforescènciaGoldPhosphorescenceLuminescenceChemistry (Weinheim an der Bergstrasse, Germany)
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SrP3N5O: a highly condensed layer phosphate structure solved from a nanocrystal by automated electron diffraction tomography.

2011

The oxonitridophosphate SrP(3)N(5)O has been synthesized by heating a multicomponent reactant mixture that consisted of phosphoryl triamide OP(NH(2))(3), thiophosphoryl triamide SP(NH(2))(3), SrS, and NH(4)Cl enclosed in evacuated and sealed silica-glass ampoules up to 750 °C. The compound was obtained as nanocrystalline powder with needle-shaped crystallites. The crystal structure was solved ab initio on the basis of electron diffraction data by means of automated electron diffraction tomography (ADT) and verified by Rietveld refinement with X-ray powder diffraction data. SrP(3)N(5)O crystallizes in the orthorhombic space group Pnma (no. 62) with unit-cell data of a=18.331(2), b=8.086(1), …

phosphatesRietveld refinementChemistryOrganic ChemistryAb initioGeneral ChemistryCrystal structureelectron diffraction; layered compounds; oxonitrides; phosphates; strontiumoxonitridesCatalysisNMR spectra databaseCrystallographyElectron diffractionlayered compoundselectron diffractionOrthorhombic crystal systemCrystallitestrontiumPowder diffractionChemistry (Weinheim an der Bergstrasse, Germany)
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Designing P-Chirogenic 1,2-Diphosphinobenzenes at Both P-Centers Using P(III)-Phosphinites

2016

International audience; A new enantiodivergent synthesis of P-chirogenic 1,2-diphosphinobenzenes (DP*B) bearing the chirality on one or both phosphorus centers is reported using aryne chemistry. The principle is based on successive reactions of 1,2-dibromobenzene with sec-phosphide boranes, then DABCO to remove the borane, and finally with chlorophosphines or P(III)-chirogenic phosphinites. The efficiency of this synthesis was demonstrated by the stereoselective preparation of (S,S)-1,2-bis(o-anisylphenylphosphino)benzene. A comparison of DIPAMP and homochiral DP*B ligands in asymmetric Rh- or Pd-catalyzed reactions was reported.

phosphine-ligandsDIPAMPketonesStereochemistryBoranesDABCOBorane010402 general chemistry[ CHIM ] Chemical Sciences01 natural sciencesBiochemistryArynecatalyzed asymmetric hydrogenationchemistry.chemical_compoundfunctionalized alkenes[ CHIM.ORGA ] Chemical Sciences/Organic chemistry[CHIM]Chemical SciencesorganocatalysisPhysical and Theoretical Chemistryhydroformylation010405 organic chemistryChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistrycarbon-monoxide0104 chemical scienceshighly enantioselective hydrogenationOrganocatalysisderivativesStereoselectivityChirality (chemistry)phospholane ligands
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